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rs1057520569

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057520569(C;T)
Make rs1057520569(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position209796375
GeneIRF6
is asnp
is mentioned by
dbSNPrs1057520569
dbSNP (old)rs1057520569
ClinGenrs1057520569
ebirs1057520569
HLIrs1057520569
Exacrs1057520569
Gnomadrs1057520569
Varsomers1057520569
Maprs1057520569
PheGenIrs1057520569
Biobankrs1057520569
1000 genomesrs1057520569
hgdprs1057520569
ensemblrs1057520569
gopubmedrs1057520569
geneviewrs1057520569
scholarrs1057520569
googlers1057520569
pharmgkbrs1057520569
gwascentralrs1057520569
openSNPrs1057520569
23andMers1057520569
23andMe allrs1057520569
SNPshotrs1057520569
SNPdbers1057520569
MSV3drs1057520569
GWAS Ctlgrs1057520569
Max Magnitude0
ClinVar
Risk rs1057520569(T;T)
Alt rs1057520569(T;T)
Reference Rs1057520569(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene IRF6
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.209969720G>A
CLNSRC
CLNACC RCV000435675.1,